Canonical Allele Identifier: PA2826418639
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr17131Ala
CA16610408
NM_001256850.1:c.51391A>G